Uterine Fibroids Increase Stroke Risk: a Mendelian Randomization Study

Abstract

Uterine fibroid, also called leiomyomas, is the most common tumor in women, affecting more than 70% of women over the age of 50. As a generally benign disease, the uterine fibroid can potentially contribute to female stroke through different pathological conditions. The relationship between uterine fibroids and stroke was occasionally reported in sporadic case reports. However, fibroids-related stroke still remains elusive at the population level. This study conducted Mendelian randomization (MR) analysis to investigate the risk of stroke (outcome) following uterine fibroid (exposure). Furthermore, through interrogating the largest clinically representative cohort of 521,612 participants, this study had sufficient power to detect the causality of uterine fibroid on different stroke subtypes, thus discovering the small vessel ischemic stroke (IS) as the most significant stroke subtype associated with uterine fibroids. In conclusion, this study explicitly indicates that uterine fibroids can causally increase the risk of stroke, rather than just a benign disease. This finding strongly suggests the importance of encompassing female populations in stroke studies and the investigation of fibroid-related stroke as a novel stroke subtype from animal models through clinical trials.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This project was supported by the National Natural Science Foundation of China (32100739) to Dr. Ming Zheng. All funding sources have been identified, and no additional funding was received for this study.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

No human subjects were directly involved in this study. All the data used in this study was derived from existing de-identified biological samples from prior studies. Thus, ethical and patient consent was not required in this study.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors.

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